Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K850020 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Gastroscope Intended to provide optical visualization of and therapeutic access to the Upper Gastro... | 2 | 06/28/2016 | Pentax Medical Company |
PENTAX Upper/Lower G.I. Endoscope OF-B130 and OF-B194 Gas/Water Feeding Valve | 2 | 08/21/2014 | Pentax Medical Company |
PENTAX Endoscopic Accessories. OF-B194. Made in Japan. PENTAX Upper/Lower G.I. Endoscopes are p... | 1 | 10/28/2013 | Pentax Medical Company |
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